5+

Product Development of Topical Dosages forms, Parenteral, Injectable forms, Tablet Dosages forms. Basic knowledge about different pharmaceutical dosage forms.

Sr. Quality Specialist, Clinical Quality responsible for managing clinical quality function, ensuring compliance with local clinical trial regulatory requirements and Takeda Quality Management Systems. Works in collaboration with local clinical operation team ensuring adherence to Good Clinical Practice Guidance.

M.Sc. Organic Chemistry, M.Pharm Pharmaceuticals Chemistry, Medicinal Chemistry, Ph.D. Organic Chemistry, Natural Product Synthesis. Experience to safety and effectively carry out routine synthetic organic chemistry techniques

Candidates must knowledge on all areas of production activities. Like handling of GLR, SSR, Centrifuge, Driers, Blender, Shifter, Miler, Documentation review, and regulatory knowledge.

Responsible to handle the team to achieve the set targets in Packaging area & maintain qualitative, quantitative as well as CGMP aspects. Knowledge of Dispensing, Sampling, Material Receiving & Issuance, SAP, Documentation.

Performs periodic follow-ups with those responsible for the implementation of CCs to ensure their completion according to the deadlines. Documents any missed deadlines. Performs the initial approvals of all CCs within the required deadlines.

Cadila Pharmaceuticals is an Indian multinational pharmaceutical company based in Ahmedabad. The company's operations focus on manufacturing products ranging from active pharmaceutical intermediates, finished formulations, food supplements, biotechnology products and pharmaceutical machinery.

Quality Control openings for BPharm, MSc at Lupin; Knowledge of HPLC, GC and others routine instruments of QC.

Expected B.Pharm, M.Pharm, M.Sc by education with 2+years experience in Injectables Validation Cleaning, process and equipment validation.